Canonical Allele Identifier: CA763930041

Gene: CRYGC

Linked Data

• dbSNP Id: rs1194186785
• gnomAD v4: 2-208129884-GA-G
• MyVariant Identifiers: chr2:g.208994609del (hg19) ; chr2:g.208129885del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.208129886del , CM000664.2:g.208129886del	GRCh38
NC_000002.11:g.208994610del , CM000664.1:g.208994610del	GRCh37
NC_000002.10:g.208702855del	NCBI36
NG_008038.1:g.4946del

Transcript Alleles

HGVS	Amino-acid Change
NR_038437.1:n.98-7170del
XM_011510661.1:c.-79-14del	XP_011508963.1:n.-79-14del
XM_011510662.1:c.-79-14del	XP_011508964.1:n.-79-14del
XM_011510663.1:c.-120-202del	XP_011508965.1:n.-120-202del